Fusia, Asian Inspirations, Kimchi & Tofu Kimbap, 8.1 OZ (230 g), Paper Film Wrapper, 12 packages per case , 6 ea: Kim
Summary
The FDA issued a Class I for Fusia, Asian Inspirations, Kimchi & Tofu Kimbap, 8.1 OZ (230 g), Paper Film Wra by GELLERT GLOBAL GROUP. Reason: Undeclared Allergen (Fish).
Details
Source
Food Recall
External ID
H-1186-2026
Action Date
2026-07-29
Status
Ongoing
Category
food
Product Description
Fusia, Asian Inspirations, Kimchi & Tofu Kimbap, 8.1 OZ (230 g), Paper Film Wrapper, 12 packages per case , 6 ea: Kimchi & Tofu Kimbap / 6 ea Spicy Tuna with Gochujang Kimbap, Keep Frozen-Do Not Thaw .
Lot/Code Info: Best if Used By: October 8, 2027
Quantity Affected: 29,850 units
Reason for Recall
Undeclared Allergen (Fish)
Distribution
The adulterated product was distributed to the following states: NY, PA, CT, NC, TX, MD
Type: Voluntary: Firm initiated
Recall Initiated: 2026-06-25
Company
Elizabeth, NJ
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 37 food recalls issued in the same week, part of 60 food-related FDA actions this month.
GELLERT GLOBAL GROUP has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (GELLERT GLOBAL GROUP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does GELLERT GLOBAL GROUP have FDA actions?
GELLERT GLOBAL GROUP has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1186-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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